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Aortic Aneurysm clinical trials

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NCT ID: NCT00597870 Completed - Clinical trials for Thoracic Aortic Dissection

Physician-Sponsored IDE for the Talent Endoluminal Stent Graft System for the Treatment of Thoracic Lesions

Start date: May 2002
Phase: N/A
Study type: Interventional

The primary objective of this trial is to determine whether the Talent Thoracic Stent Graft, an investigational device, is a safe and effective method of treating thoracic aortic aneurysms (abnormal ballooning of the vessel wall) and other thoracic lesions (dissections, transections, pseudoaneurysms, penetrating ulcers, etc.). The endovascular method is a substitute for the major operation that is performed to treat the lesions.

NCT ID: NCT00593814 Completed - Clinical trials for Aortic Aneurysm, Abdominal

GORE EXCLUDER® Endoprosthesis - Low Permeability in Treatment of Abdominal Aortic Aneurysms

Start date: June 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the performance of the GORE EXCLUDER® Bifurcated Endoprosthesis-Low Permeability in the primary treatment of infrarenal abdominal aortic aneurysms.

NCT ID: NCT00591968 Completed - Clinical trials for Abdominal Aortic Aneurysm

Telesonography Adaptation and Use to Improve the Standard of Patient Care Within a Dominican Community

Start date: January 2008
Phase: N/A
Study type: Interventional

The role of teleradiology has far reaching implications for the health of remote and underserved populations. The ability to coordinate radiographic evaluation and diagnosis from a distance has the potential to raise the standard of patient care throughout the world. Perhaps the safest and most cost effective mode of teleradiology today is telesonography. The current project attempts to determine the extent that telesonography improves the standard of care within a rural government-run primary clinic within the Dominican Republic. The work reported herein is intended to compare the use of telesonography to the current standard of sonographic examination (referral to government hospital 60km from target clinic). The study was conducted by randomly assigning 100 patients with clinical indications for sonographic examination into experimental and control groups. Following a 60-day implementation period, the following research questions will be addressed: 1) To what extent does the use of asynchronous telesonography increase the percentage of definitive diagnoses based on the total number of scans (definitive diagnoses / total number of scans)? 2) To what extent does the use of asynchronous telesonography increase the continuity of care for patients? 3) To what extent does the elapsed time between scanning and final radiological interpretation decrease with the use of asynchronous telesonography? This study will also look at the history of telemedicine / telesonography and its dissemination into the mainstream practice of medicine, explore training protocols that may be used to assist others to establish new telesonography programs in a developing nations, and discuss both advances and persistent barriers to the implementation of telesonography programs. Hypothesis: The use of a store-and-forward telesonography system in this setting will increase the speed and number of final diagnoses per scan received by the target clinic and will increase the continuity of care by increasing the number and speed of follow-up appointments to the target clinic.

NCT ID: NCT00590759 Completed - Clinical trials for Aortic Aneurysm, Thoracic

Evaluation of the GORE TAG Thoracic Endoprosthesis in the Treatment of Aneurysms

Start date: August 2005
Phase: N/A
Study type: Interventional

The purpose of this post-approval study is to evaluate the long-term performance of the GORE TAG® Thoracic Endoprosthesis (TAG device) in the primary treatment of descending thoracic aortic (DTA) aneurysms

NCT ID: NCT00587977 Completed - Clinical trials for Abdominal Aortic Aneurysm

Aortic Distensibility

FAMRI
Start date: November 2004
Phase: N/A
Study type: Observational

Can software be developed to automatically aid in the measurement of abdominal aortic aneurysms, and is there a way to predict future rupture or growth of abdominal aortic aneurysms.

NCT ID: NCT00583817 Enrolling by invitation - Aortic Dissection Clinical Trials

Endovascular Treatment of Thoracic Aortic Disease

EVOLVE Aorta
Start date: October 25, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the role endovascular therapy to treat aortic disease involving the ascending aorta, the aortic arch, and the visceral segment of the aorta (or thoracoabdominal aorta)

NCT ID: NCT00583414 Completed - Clinical trials for Abdominal Aortic Aneurysm

Endovascular Exclusion of Abdominal Aortic Aneurysms in High Risk Patients

Start date: September 1998
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the role of abdominal aneurysm and iliac aneurysm exclusion using an endovascular prosthesis.

NCT ID: NCT00583050 Completed - Clinical trials for Abdominal Aortic Aneurysm

Endovascular Exclusion of TAAA/AAA Utilizing Fenestrated/Branched Stent Grafts

Start date: February 2001
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the role of fenestrated/branched stent-grafts in the exclusion of abdominal aortic and thoracoabdominal aneurysms.

NCT ID: NCT00549432 Active, not recruiting - Clinical trials for Abdominal Aortic Aneurysm

Clinical Study of Abdominal Aortic Aneurysm Exclusion (TALENT Abdominal)

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Start date: October 2002
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the TALENT endoluminal stent-graft system in patients with abdominal aortic aneurysms. The TALENT endoluminal stent-graft system is a flexible, implantable endoluminal vascular device preloaded in a placement system that is used to exclude abdominal aortic aneurysms.

NCT ID: NCT00549354 Active, not recruiting - Aortic Aneurysm Clinical Trials

Abdominal Aortic/Aorto-Iliac Aneurysm Endoluminal Graft Study

Start date: August 2000
Phase: Phase 2
Study type: Interventional

The Bifurcated PowerLink System is intended to provide a permanent alternative conduit for blood flow within a patient's abdominal vascular system, which excludes the aneurysmal sac from blood flow and pressure.